@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP515998.RAPthLWAMBclP7XDNfSrGboV62wRULwccFe1o0wVARTK0
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP515998.RAPthLWAMBclP7XDNfSrGboV62wRULwccFe1o0wVARTK0130_head
{
this:
np:hasAssertion
dgn-np:NP515998.RAPthLWAMBclP7XDNfSrGboV62wRULwccFe1o0wVARTK0130_assertion
;
np:hasProvenance
dgn-np:NP515998.RAPthLWAMBclP7XDNfSrGboV62wRULwccFe1o0wVARTK0130_provenance
;
np:hasPublicationInfo
dgn-np:NP515998.RAPthLWAMBclP7XDNfSrGboV62wRULwccFe1o0wVARTK0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP515998.RAPthLWAMBclP7XDNfSrGboV62wRULwccFe1o0wVARTK0130_assertion
a
np:Assertion
.
dgn-np:NP515998.RAPthLWAMBclP7XDNfSrGboV62wRULwccFe1o0wVARTK0130_provenance
a
np:Provenance
.
dgn-np:NP515998.RAPthLWAMBclP7XDNfSrGboV62wRULwccFe1o0wVARTK0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP515998.RAPthLWAMBclP7XDNfSrGboV62wRULwccFe1o0wVARTK0130_assertion
{
miriam-gene:4436
a
ncit:C16612
.
lld:C0009402
a
ncit:C7057
.
dgn-gda:DGNbbb653c0ba5c4b8206d14d63a29ce8f7
sio:SIO_000628
miriam-gene:4436
,
lld:C0009402
;
a
sio:SIO_001121
.
}
dgn-np:NP515998.RAPthLWAMBclP7XDNfSrGboV62wRULwccFe1o0wVARTK0130_provenance
{
dgn-np:NP515998.RAPthLWAMBclP7XDNfSrGboV62wRULwccFe1o0wVARTK0130_assertion
dcterms:description
"[We tested 538 patients for p53 codon 72 variants, including 167 unrelated patients with pathogenic germline mutations in MSH2 or MLH1 and colorectal carcinoma as first tumour, 126 patients with sporadic microsatellite stable colorectal cancers, and 245 healthy controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:16199549
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP515998.RAPthLWAMBclP7XDNfSrGboV62wRULwccFe1o0wVARTK0130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:38+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetv3.0rdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}